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Article

Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic teleangiectasia and anemia.

European journal of gastroenterology & hepatology - 1 Feb 2007

van Tuyl Sebastiaan A C, Letteboer Tom G W, Rogge-Wolf Claudia, Kuipers Ernst J, Snijder Repke J, Westermann Cees J J, Stolk Mark F J

Abstract excerpt

INTRODUCTION: Hereditary hemorrhagic teleangiectasia (HHT) is an autosomal dominant disorder with mucocutaneous teleangiectasia and visceral arteriovenous malformations. Mutations of endoglin and Activin A receptor like kinase-1 have different phenotypes, HHT1 and HHT2, respectively. The gastrointestinal tract is frequently affected, but limited information is available on the relationship with genotype. AIM: To...

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Identifiers

PMID: 17273001
DOI: 10.1097/01.meg.0000252633.88419.04

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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